A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046496



Internal ID98805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60805107..60806923hg38UCSC Ensembl
chr11:60572580..60574396hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381817
hg191817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497467
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046496
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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